Associate Director, Clinical Trial Management

Overview The Associate Director, Clinical Trial Management role supports the execution, and management of clinical trials to ensure they meet regulatory requirements, timelines, and quality standards. You will support cross-functional teams, liaise and oversee clinical research organizations (CROs), and ensure that trials are conducted efficiently and ethically while maintaining patient safety. This position reports to the Executive Director, Clinical Operations. Key Responsibilities Support the planning, initiation, execution, and closeout of clinical trials. Coordinate clinical trial operational activities to ensure completion according to project timelines and budget. Ensure clinical trials are conducted in compliance with NewAmsterdam Pharma SOPs, GCP/ICH and other regulatory requirements and work cooperatively with Quality Assurance regarding site audits. Manage and review clinical trial documentation, including protocols, informed consent forms, study plans, and reports. Ensure the collection, management, and reporting of clinical trial data meets the highest standards of quality. Identify and resolve issues related to trial data, patient recruitment and retention, and site performance. Manage clinical trial timelines, enrollment and patient retention objectives in support of trial execution. Support cross‑functional teams including representatives from multiple disciplines (e.g. Regulatory Affairs, CMC, etc.). Review and oversee clinical trial regulatory packages prepared by the CRO in support of submissions to regulatory authorities and ethics committees. Oversee vendor and CRO activities and track internal and external (CRO/vendor) project deliverables to ensure they remain within the timeline and budget. Support the construction and maintenance of the trial master file (TMF) with vendors and assure completeness and successful transfer from vendor to NewAmsterdam Pharma. Stay current with regulations and industry trends and provide input into processes to ensure adherence to regulations and best practice standards. Actively communicate project issues and identify emerging risks, then work with the internal team to resolve challenges. Assist in the development of standard operating procedures. Qualifications Bachelor’s degree in a scientific discipline, RN, or equivalent. PMP preferred. 5+ years Phase 1-3 global clinical trial operations experience. Demonstrated experience managing external vendors/CROs. Experience in cardiovascular disease strongly preferred. Demonstrated self‑discipline, motivation, and entrepreneurial ability. Advanced knowledge of GCP, ICH and FDA regulatory requirements. Ability to continuously re‑prioritize and work independently as a member of a cross‑functional team and with external vendors with minimal supervision. Ability to effectively collaborate with cross‑functional teams. Excellent interpersonal, oral, written communication skills. Proficiency with clinical trial management systems (CTMS) and other related software. Proficient in MS Office (e.g., Outlook, Word, PowerPoint, Excel). Salary and Benefits We offer a competitive base salary, an annual bonus, and long‑term incentives. In addition, we provide a comprehensive benefits package, including health insurance, dental and vision coverage, term life and disability coverage, and retirement plans. EEO Statement NewAmsterdam Pharma is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information, or any other basis protected by federal, state or local law. #J-18808-Ljbffr